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In-vitro bioequivalence study of 8 brands of metformin tablets in Iran market

Parvin Zakeri-Milani, Peyman Nayyeri-Maleki, Saeed Ghanbarzadeh, Mahboob Nemati, Hadi Valizadeh

DOI: 10.7324/JAPS.2012.2834Pages: 194-197

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Design of dissolution media for in-vitro bioequivalence testing of Lamivudine

Nagiat T Hwisa, Shanta Kumari Adiki, Prakash Katakam, Babu Rao Chandu

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Model-Based Bioequivalence assessment of a commercial Azithromycin Capsule against Pfizer Zithromax® Tablet marketed in Jamaica

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DOI: 10.7324/JAPS.2014.401012Pages: 062-068

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Study of regulatory requirements for the conduct of bioequivalence studies in US, Europe, Canada, India, ASEAN and SADC countries: Impact on generic drug substitution

Nitika Kaushal, Sachin Kumar Singh, Monica Gulati, Yogyata Vaidya, Munish Kaushik

DOI: 10.7324/JAPS.2016.60430Pages: 206-222

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Bioequivalence regulation in emerging countries: Example of Moroccan regulations on immediate release formulations and comparison with international guidelines

Casimir Adade Adade, Amine Cheikh, Yahia Cherrah, Mustapha Bouatia, Jean Michel Cardot

DOI: 10.7324/JAPS.2019.91104Pages: 028-035

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Factors affecting purchasing behaviors of generic drugs versus originator counterparts in Jordan

Maha N. Abu Hajleh, Ali AL-Samydai, Zahraa Aloosi, Raghad Abuhamdan, Sumaiah Al.Naimat, Lina Abdelfattah, Lidia Al-Halaseh

DOI: 10.7324/JAPS.2021.110902Pages: 009-017

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